GetGRangesWindowSeqandParam | R Documentation |
Return the GRanges object provided with the sequence associated to each position (and can also retrieve the sequence around each position).
GetGRangesWindowSeqandParam( grangesData, grangesGenome, dnastringsetGenome, nUpstreamBpToAdd = 0, nDownstreamBpToAdd = 0 )
grangesData |
A GRanges object containing Modifications Positions data to be extracted with the sequence. |
grangesGenome |
A GRanges object containing the width of each contig. |
dnastringsetGenome |
A DNAStringSet object containing the sequence for each contig. |
nUpstreamBpToAdd |
Number of base pairs to add upstream of the range from the GRanges object provided to obtain some sequence upstream of range. If some new ranges do not fit in the ranges of the contigs (provided with grangesGenome), those new ranges will be removed. New windows with gaps are also removed. Defaults to 0. |
nDownstreamBpToAdd |
Number of base pairs to add downstream of the range from the GRanges object provided to obtain some sequence downstream of range. If some new ranges do not fit in the ranges of the contigs (provided with grangesGenome), those new ranges will be removed. New windows with gaps are also removed. Defaults to 0. |
# loading genome myGenome <- Biostrings::readDNAStringSet(system.file( package = "DNAModAnnot", "extdata", "ptetraurelia_mac_51_sca171819.fa" )) myGrangesGenome <- GetGenomeGRanges(myGenome) # Preparing a grangesPacBioGFF datasets myGrangesPacBioGFF <- ImportPacBioGFF( cPacBioGFFPath = system.file( package = "DNAModAnnot", "extdata", "ptetraurelia.modifications.sca171819.gff" ), cNameModToExtract = "m6A", cModNameInOutput = "6mA", cContigToBeAnalyzed = names(myGenome) ) # Retrieve GRanges with sequence myPositions_Mod_Granges_wSeq <- GetGRangesWindowSeqandParam( grangesData = myGrangesPacBioGFF, grangesGenome = myGrangesGenome, dnastringsetGenome = myGenome, nUpstreamBpToAdd = 5, nDownstreamBpToAdd = 5 ) myPositions_Mod_Granges_wSeq
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